Taiwan FDA registration d06d98e9e361bbcd21a4f18a8182a922
“Stryker” CrossFlow Integrated Arthroscopy Pump
TW: “史賽克”整合關節鏡幫浦
Taiwan·Risk Class 2·MD·STRYKER ENDOSCOPY·Registered Oct 31, 2022 – Oct 31, 2027ActiveRegistration details
- Analysis ID
- d06d98e9e361bbcd21a4f18a8182a922
- License Form
- Ministry of Health Medical Device Import No. 036016
- Customs Code
- DHA05603601603
Company information
- Manufacturer
- STRYKER ENDOSCOPY
- Manufacturer Country
- United States
- Authorized Representative
- Stryker (Far East) Co., Ltd. Taiwan Branch
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N1100 Arthroscopy
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 31, 2022
- Expiry Date
- Oct 31, 2027
About this record
Access comprehensive regulatory information for “Stryker” CrossFlow Integrated Arthroscopy Pump in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d06d98e9e361bbcd21a4f18a8182a922 and manufactured by STRYKER ENDOSCOPY. The authorized representative in Taiwan is Stryker (Far East) Co., Ltd. Taiwan Branch.
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